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1.
J Pediatr ; 206: 286-292.e1, 2019 03.
Article in English | MEDLINE | ID: mdl-30413314

ABSTRACT

Variable lung disease was documented in 2 infants with heterozygous TBX4 mutations; their clinical presentations, pathology, and outcomes were distinct. These findings demonstrate that TBX4 gene mutations are associated with neonatal respiratory failure and highlight the wide spectrum of clinicopathological outcomes that have implications for patient diagnosis and management.


Subject(s)
Mutation/genetics , Respiratory Insufficiency/genetics , Respiratory Insufficiency/pathology , T-Box Domain Proteins/genetics , Female , Humans , Infant, Newborn , Male
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